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Changes in the mesenteric lymph proteome induced by hemorrhagic shock.

机译:肠系膜淋巴蛋白质组的变化引起的出血性休克。

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摘要

Biologically active factors produced by the intestine and transported by the aqueous and protein fraction of mesenteric lymph are now thought to contribute significantly to the development of distant organ failure in hemorrhagic shock. Despite the likely relevance of the protein composition of mesenteric lymph conditioned by hemorrhagic shock, there is no detailed description of its proteome. The aim of this study was to provide the first comprehensive description of the proteome of hemorrhagic shock-conditioned mesenteric lymph. Mesenteric lymph was collected from 16 male Wistar rats randomized to group 1 (n = 8) sham control and group 2 (n = 8) with hemorrhagic shock. The lymph was subjected to proteomic analysis using iTRAQ and liquid chromatography-tandem mass spectrometry. Sixty of the 245 proteins had a significant increase in their relative abundance in the hemorrhagic shock group. A bioinformatics approach highlighted the importance of the key gene ontology pathways relating to response to injury and metabolic responses as changing most significantly in shock. Using an interactome, we identified several highly connected proteins: 14-3-3 Zeta, 14-3-3 epsilon, actin, aldolase A, calmodulin, cofilin 1, cystatin C, fatty acid-binding protein 4, profilin 1, prolyl 4-hydrolase, peptidylprolyl isomerase, and transgelin. This study provides the first detailed description of protein changes in hemorrhagic shock-conditioned mesenteric lymph, and using a bioinformatics approach, we identified several targets for possible further research.
机译:生物活性因素产生的由水和肠和运输蛋白质的肠系膜淋巴现在想做出显著贡献遥远的器官衰竭的发展出血性休克。肠系膜淋巴结的蛋白质组成受制于出血性休克,没有蛋白质组的详细描述。本研究旨在提供第一个全面出血性的蛋白质组的描述shock-conditioned肠系膜淋巴。淋巴收集来自16个雄性Wistar鼠随机分配到组1 (n = 8)和虚假的控制第二组(n = 8)与出血性休克。是进行蛋白质组学分析使用iTRAQ和液体chromatography-tandem质量谱分析。显著增加它们的相对丰度出血性休克组。方法强调关键的重要性基因本体通路相关回应损伤和代谢反应的改变大幅冲击。确定几个高度连接蛋白:14-3-3ζ,14-3-3ε、肌动蛋白、醛缩酶,钙调蛋白,cofilin 1,半胱氨酸蛋白酶抑制物C,脂肪结合蛋白4,prolyl profilin 1日4-hydrolase、peptidylprolyl异构酶transgelin。详细描述蛋白质的变化出血性shock-conditioned肠系膜淋巴结,我们使用生物信息学方法,进一步确定了几个目标可能研究。

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